BackChapter 10: Blood – Structure, Function, and Clinical Relevance
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Blood: Composition and Functions
Overview of Blood
Blood is the only fluid tissue in the human body and is classified as a connective tissue. It plays a vital role in transporting substances, regulating physiological parameters, and protecting the body against disease.
Components of Blood:
Formed elements (living cells): erythrocytes, leukocytes, and platelets
Plasma (non-living matrix): the liquid portion containing dissolved substances
Physical Characteristics of Blood
Color: Oxygen-rich blood is scarlet red; oxygen-poor blood is dull red.
pH: Must remain between 7.35–7.45 for proper physiological function.
Volume: In a healthy adult male, blood volume is about 5–6 liters (6 quarts), making up approximately 8% of body weight.
Blood Composition After Centrifugation
Erythrocytes (RBCs): Settle at the bottom (45% of blood, known as the hematocrit).
Buffy coat: Thin, whitish layer between erythrocytes and plasma; contains leukocytes and platelets (<1% of blood).
Plasma: Rises to the top (55% of blood).
Blood Plasma
Composition and Functions
Blood plasma is a straw-colored, sticky fluid that makes up about 55% of blood volume. It is composed of approximately 90% water and contains a variety of dissolved substances.
Nutrients: Glucose, amino acids, fatty acids, vitamins
Salts (Electrolytes): Sodium, potassium, calcium, magnesium, chloride, bicarbonate
Respiratory Gases: Oxygen and carbon dioxide
Hormones
Plasma Proteins: Albumin, clotting proteins, antibodies
Waste Products: Urea, uric acid, creatinine
Plasma Proteins
Albumin: Regulates osmotic pressure, maintaining blood volume and pressure.
Clotting Proteins: Help stem blood loss when a blood vessel is injured (e.g., fibrinogen, prothrombin).
Antibodies (Immunoglobulins): Protect the body from pathogens.
Formed Elements of Blood
Overview
Erythrocytes (Red Blood Cells, RBCs): Specialized for oxygen transport.
Leukocytes (White Blood Cells, WBCs): Crucial for immune defense.
Platelets (Thrombocytes): Cell fragments essential for blood clotting.
Table: Characteristics of Formed Elements of the Blood
Cell Type | Occurrence in Blood (per mm3) | Cell Anatomy | Function |
|---|---|---|---|
Erythrocytes (RBCs) | 4–6 million | Biconcave, anucleate, essentially bags of hemoglobin | Transport oxygen bound to hemoglobin; small amount of CO2 transport |
Leukocytes (WBCs) | 4,000–11,000 | Complete cells with nucleus and organelles | Defense against disease |
Platelets | 150,000–400,000 | Cell fragments from megakaryocytes | Needed for blood clotting |
Erythrocytes (Red Blood Cells)
Main Function: Carry oxygen from the lungs to tissues.
Structure: Biconcave disks, anucleate, very few organelles, filled with hemoglobin.
Hemoglobin: Iron-containing protein; each molecule binds up to four oxygen molecules. Each RBC contains about 250 million hemoglobin molecules.
Normal Hemoglobin Content: 12–18 g per 100 mL of blood.
Homeostatic Imbalances of RBCs
Anemia: Decreased oxygen-carrying capacity of blood due to low RBC count or abnormal hemoglobin.
Sickle Cell Anemia (SCA): Genetic disorder causing abnormally shaped hemoglobin, leading to sickle-shaped RBCs.
Polycythemia: Excessive or abnormal increase in RBC number, increasing blood viscosity.
Table: Types of Anemia
Direct Cause | Resulting From | Leading To |
|---|---|---|
Decrease in RBC number | Hemorrhage, hemolysis, lack of vitamin B12, destruction of bone marrow | Hemorrhagic, hemolytic, pernicious, aplastic anemia |
Inadequate hemoglobin content in RBCs | Lack of iron or slow/bleeding ulcers | Iron-deficiency anemia |
Abnormal hemoglobin in RBCs | Genetic defects (e.g., sickle cell gene) | Sickle cell anemia |
Leukocytes (White Blood Cells)
Function: Crucial in defense against disease; can move in and out of blood vessels (diapedesis) and respond to tissue damage.
Normal Count: 4,000–11,000 per mm3 of blood.
Abnormal Numbers:
Leukocytosis: WBC count above 11,000/mm3, usually indicates infection.
Leukopenia: Abnormally low WBC count, often due to drugs.
Leukemia: Cancerous bone marrow produces excess, abnormal WBCs.
Types of Leukocytes
Granulocytes: Contain granules in cytoplasm, lobed nuclei.
Neutrophils: Phagocytes at infection sites.
Eosinophils: Respond to allergies and parasitic worms.
Basophils: Contain histamine; initiate inflammation.
Agranulocytes: Lack visible granules, nuclei are spherical/oval/kidney-shaped.
Lymphocytes: Important in immune response (B and T cells).
Monocytes: Largest WBCs; become macrophages, fight chronic infection.
Relative Abundance of WBCs
Neutrophils > Lymphocytes > Monocytes > Eosinophils > Basophils
Mnemonic: Never Let Monkeys Eat Bananas
Platelets
Origin: Derived from ruptured megakaryocytes (large multinucleate cells).
Function: Essential for blood clotting (hemostasis).
Normal Count: 150,000–400,000 per mm3 (average 300,000/mm3).
Blood Groups and Transfusions
Importance of Blood Groups
Blood transfusions are critical for replacing lost blood, but compatibility is essential to prevent immune reactions. Blood groups are determined by genetically inherited antigens on RBC surfaces.
Major Blood Groups: ABO and Rh systems
Antigens: Substances recognized as foreign by the immune system; can trigger antibody production.
Antibodies: Proteins that recognize and bind to specific antigens, causing agglutination (clumping) if incompatible blood is transfused.
Table: ABO Blood Groups
Blood Group | RBC Antigens | Plasma Antibodies | Blood That Can Be Received |
|---|---|---|---|
AB | A, B | None | A, B, AB, O (Universal recipient) |
B | B | Anti-A | B, O |
A | A | Anti-B | A, O |
O | None | Anti-A, Anti-B | O (Universal donor) |
ABO Blood Group System
Type AB: Both A and B antigens; no anti-A or anti-B antibodies; universal recipient.
Type A: A antigen; anti-B antibodies.
Type B: B antigen; anti-A antibodies.
Type O: No antigens; both anti-A and anti-B antibodies; universal donor.
Rh Blood Group System
Rh Antigen (D): Presence (+) or absence (−) of Rh antigen on RBCs.
Most Americans are Rh positive (Rh+).
Transfusion Reaction: Mixing Rh+ blood into an Rh− recipient can cause immune complications.
Rh Dangers During Pregnancy
Occurs when an Rh− mother carries an Rh+ fetus.
First pregnancy usually proceeds without problems; the mother becomes sensitized.
In subsequent pregnancies, maternal anti-Rh antibodies can attack fetal RBCs, causing hemolytic disease of the newborn.
Prevention: RhoGAM injection prevents maternal sensitization.
Blood Typing and Cross-Matching
Blood Typing Procedure
Blood samples are mixed with anti-A and anti-B sera.
Coagulation (agglutination) indicates the presence of the corresponding antigen.
Typing for ABO and Rh factors is performed similarly.
Cross-matching tests for agglutination of donor RBCs by recipient serum and vice versa.
Example: Blood Typing Results
Type AB: Agglutinates with both anti-A and anti-B sera.
Type A: Agglutinates with anti-A serum only.
Type B: Agglutinates with anti-B serum only.
Type O: No agglutination with either serum.
Summary Table: Blood Groups, Antigens, Antibodies, and Compatibility
Blood Type | Antigens on RBCs | Antibodies in Plasma | Can Donate To | Can Receive From |
|---|---|---|---|---|
A | A | Anti-B | A, AB | A, O |
B | B | Anti-A | B, AB | B, O |
AB | A, B | None | AB | All types |
O | None | Anti-A, Anti-B | All types | O |
Key Equations and Concepts
Hematocrit: Percentage of RBCs in total blood volume.
Clinical Application Example
Blood Transfusion: A patient with type B blood can safely receive type B or type O blood, but not type A or AB, to avoid agglutination and transfusion reactions.
Hemolytic Disease of the Newborn: Prevented by administering RhoGAM to Rh− mothers after delivery of an Rh+ baby.
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